Pharmaceutical Manufacturing seeks a Regulatory Affairs Associate.  Resp. include creating & implementing labels for OTC & ANDA submissions, assist in ANDA submissions using eCTD submission software, prepare & maintain annual reports, SOP, deviations & OOS reports, review product complaints & queries & support in developing regulatory strategies & launch OTC products.  Applicant must possess a Master’s Degree in Pharmaceutical Manufacturing/Pharmacy/Pharmacy Administration/Regulatory Affairs and Quality Assurance w/6 months of exp.  40 hrs/wk M-F.  Mail or Submit Resumes ref. to job # SP001 Sunrise Pharmaceuticals Inc. 665 East Lincoln Ave., Rahway, NJ 07065.